Sequence Ontology

A shared vocabulary for biological sequence features and annotations

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MNV

SO:0002007

Definition: An MNV is a multiple nucleotide variant (substitution) in which the inserted sequence is the same length as the replaced sequence.

Comments and references

Definition references: NCBI:th

Synonyms

ScopeValue
exactmultiple nucleotide substitution
exactmultiple nucleotide variant

Identifiers and subsets

Accession: SO:0002007

Persistent URL: http://purl.obolibrary.org/obo/SO_0002007

Alternate IDs: None

Subsets: None

Cross references: None

History summary

Term history is reconstructed from the Git-era ontology files by comparing ontology classes across revisions. Earlier SVN-era changes will be added at a future date.

First seen in Git-era editable history: 2016-12-05 in commit 92e3cae

Most recent Git-era change: 2016-12-05 in commit 92e3cae

Number of changes: 1

Ontology neighborhood diagram

Ontology neighborhood for SO:0002007 Ontology neighborhood graph for SO:0002007 MNV. Parent, child, and related nodes can be activated to open their term pages. SO:1000002 substitution SO:1000002 substitution SO:0002007 MNV SO:0002007 MNV SO:0001013 MNP SO:0001013 MNP
The local DAG shows nearby parent, child, and related terms. Each node links to its own term page.

Relationships

Parents

Children

Change history

This timeline summarizes changes identified in SO’s GitHub commit history, including updates to labels, definitions, parent terms, synonyms, subsets, and obsoletion status. It is a best-effort reconstruction and may not include every change to a term. Since only history from GitHub is included at the moment, any term added before the migration from SVN to Git will show as being created in 2016. This will be addressed once SVN history is incorporated.

DateChangeSummaryEvidence
2016-12-05createdTerm introduced into the editable ontology history
Initial label: MNV
Initial definition captured.
Initial parent: SO:1000002
92e3cae